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EC number: 696-616-8 | CAS number: 1268344-02-0
- Life Cycle description
- Uses advised against
- Endpoint summary
- Appearance / physical state / colour
- Melting point / freezing point
- Boiling point
- Density
- Particle size distribution (Granulometry)
- Vapour pressure
- Partition coefficient
- Water solubility
- Solubility in organic solvents / fat solubility
- Surface tension
- Flash point
- Auto flammability
- Flammability
- Explosiveness
- Oxidising properties
- Oxidation reduction potential
- Stability in organic solvents and identity of relevant degradation products
- Storage stability and reactivity towards container material
- Stability: thermal, sunlight, metals
- pH
- Dissociation constant
- Viscosity
- Additional physico-chemical information
- Additional physico-chemical properties of nanomaterials
- Nanomaterial agglomeration / aggregation
- Nanomaterial crystalline phase
- Nanomaterial crystallite and grain size
- Nanomaterial aspect ratio / shape
- Nanomaterial specific surface area
- Nanomaterial Zeta potential
- Nanomaterial surface chemistry
- Nanomaterial dustiness
- Nanomaterial porosity
- Nanomaterial pour density
- Nanomaterial photocatalytic activity
- Nanomaterial radical formation potential
- Nanomaterial catalytic activity
- Endpoint summary
- Stability
- Biodegradation
- Bioaccumulation
- Transport and distribution
- Environmental data
- Additional information on environmental fate and behaviour
- Ecotoxicological Summary
- Aquatic toxicity
- Endpoint summary
- Short-term toxicity to fish
- Long-term toxicity to fish
- Short-term toxicity to aquatic invertebrates
- Long-term toxicity to aquatic invertebrates
- Toxicity to aquatic algae and cyanobacteria
- Toxicity to aquatic plants other than algae
- Toxicity to microorganisms
- Endocrine disrupter testing in aquatic vertebrates – in vivo
- Toxicity to other aquatic organisms
- Sediment toxicity
- Terrestrial toxicity
- Biological effects monitoring
- Biotransformation and kinetics
- Additional ecotoxological information
- Toxicological Summary
- Toxicokinetics, metabolism and distribution
- Acute Toxicity
- Irritation / corrosion
- Sensitisation
- Repeated dose toxicity
- Genetic toxicity
- Carcinogenicity
- Toxicity to reproduction
- Specific investigations
- Exposure related observations in humans
- Toxic effects on livestock and pets
- Additional toxicological data
Short-term toxicity to aquatic invertebrates
Administrative data
Link to relevant study record(s)
- Endpoint:
- short-term toxicity to aquatic invertebrates
- Type of information:
- read-across from supporting substance (structural analogue or surrogate)
- Adequacy of study:
- supporting study
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: Guideline study, GLP, All validity criteria fulfilled, complete identification of test substance, including chemical analyses
- Justification for type of information:
- REPORTING FORMAT FOR THE ANALOGUE APPROACH
The short term toxicity test result as observed for the tallow based product is read across to the Oleyl based product. The products differ only in their alkylchain distribution. Both tallow and Oleyl are natural fats for which the composition slightly changes over time due to changes in the environmental considitions.
The tallow alkyl fat which is used for the production of CAS no 1268344-02-0 are for 99 % straight chain alkyl fats
Commercial tallow alkyl fats have the following distribution:
C12 about 2 %
C14 about 4 %
C16 about 31 %
C18 about 65 %,
where 40 –50 % are unsaturated.
The oleyl fate which is used for the production of CAS no 1290049-56-7 are also straight chain fates
Commercial Oleylfats have the following distribution:
C12 1 %
C14 2 - 4 %
C16 and C16’ 12 - 14 %
C18, C18’ and C18’’ > 80 % (C18: 8 %, C18’cis: 46 %, C18’trans: 21 %, C18’’: 5 %)
C20 1 %
(a single prime indicates one double bond, a double prime indicates two double bonds):
When the water solubility of cationic surfactants based on tallow are compared to oleyl based cationic surfactants it is consistently the tallow product which has a sligthly lower water solubility and due to that also a slightly lower bioavailability. This lower bioavailability regularly results is slight differences in biodegradation rate and ecotoxicity. The substances are however difficult to test substances and the variation in the test results is especially in ecotoxicity testing frequently larger than the difference in bioavailability. It is therefore considered justified to use the tallow product test results for read across for the oleyl based product. - Reason / purpose for cross-reference:
- read-across source
- Qualifier:
- according to guideline
- Guideline:
- other: OECD TG 211
- Deviations:
- no
- GLP compliance:
- yes (incl. QA statement)
- Test organisms (species):
- Daphnia magna
- Test type:
- semi-static
- Water media type:
- freshwater
- Limit test:
- no
- Reference substance (positive control):
- no
- Duration:
- 21 d
- Dose descriptor:
- EC50
- Effect conc.:
- 421 µg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mobility
Reference
Description of key information
Short term (48-h) toxicity to Daphnia magna was investigated in accordance with the guideline OECD 202 with a tallow based ethoxylated diamine but without confirmation of the exposure concentrations by chemical analysis. To support the use of this tallow based result for read-across to the oleyl based ethoxylated diamine without additional safety factor, the 21d-EC50 for parental mortality of 421 µg/L as observed for the oleyl based ethoxylated diamine is included to the information used to evaluate the acute effects on daphnia. The lowest value will as a worst-case be used for risk assessment.
Key value for chemical safety assessment
Fresh water invertebrates
Fresh water invertebrates
- Effect concentration:
- 0.31 mg/L
Additional information
The short-term tests on toxicity to Daphnia magna were conducted in a period when no reliable specific method of analyses was available. The concentrations were therefore not analytically verified, the reliability of the results is therefore limited.
Information on Registered Substances comes from registration dossiers which have been assigned a registration number. The assignment of a registration number does however not guarantee that the information in the dossier is correct or that the dossier is compliant with Regulation (EC) No 1907/2006 (the REACH Regulation). This information has not been reviewed or verified by the Agency or any other authority. The content is subject to change without prior notice.
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